4.8 Article

The nuclear receptor HNF4 drives a brush border gene program conserved across murine intestine, kidney, and embryonic yolk sac

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-021-22761-5

Keywords

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Funding

  1. NIH [R01CA190558, R01DK121915, R01DK112782]
  2. New Jersey Commission on Cancer Research grant [DFHS18PPC051]
  3. Sequencing Facility and Metabolomics Shared Resource of the Rutgers Cancer Institute of New Jersey [P30CA072720]
  4. imaging core facility of Human Genetics Institute of New Jersey
  5. MacMillan Summer Undergraduate Research Fellowships
  6. Intestinal Stem Cell Consortium from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the National Institutes of Health [U01 DK103141]
  7. Intestinal Stem Cell Consortium from National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health [U01 DK103141]

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The brush border is a specialized structure on the apical surface of epithelia that greatly increases absorptive surface area, but the transcriptional regulatory networks controlling brush border genes are not fully understood. This study identifies HNF4 as a conserved regulator of the brush border gene program in multiple organs, such as intestine, kidney, and yolk sac, and reveals its role in chromatin looping between promoters and enhancers in the intestine.
The brush border is comprised of microvilli surface protrusions on the apical surface of epithelia. This specialized structure greatly increases absorptive surface area and plays crucial roles in human health. However, transcriptional regulatory networks controlling brush border genes are not fully understood. Here, we identify that hepatocyte nuclear factor 4 (HNF4) transcription factor is a conserved and important regulator of brush border gene program in multiple organs, such as intestine, kidney and yolk sac. Compromised brush border gene signatures and impaired transport were observed in these tissues upon HNF4 loss. By ChIP-seq, we find HNF4 binds and activates brush border genes in the intestine and kidney. H3K4me3 HiChIP-seq identifies that HNF4 loss results in impaired chromatin looping between enhancers and promoters at gene loci of brush border genes, and instead enhanced chromatin looping at gene loci of stress fiber genes in the intestine. This study provides comprehensive transcriptional regulatory mechanisms and a functional demonstration of a critical role for HNF4 in brush border gene regulation across multiple murine epithelial tissues. Brush border gene regulation in various different tissues is incompletely understood. Here, the authors show HNF4 regulates the brush border gene program in multiple organs, such as intestine, kidney and yolk sac, and also intestinal chromatin looping in these tissues between promoters and enhancers.

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